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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2265092Generated: October 28, 2026

p-Nitroacetophenone → HCID 11031413, compound

https://huagongshe.com/reaction/2265092

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-NitroacetophenoneHCID 7487—
ReactantAmmonium ChlorideHCID 25517—
Reactant18-Crown-6HCID 28557—
ReactantTrimethyl phosphonoacetateHCID 80029—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
SolventTolueneHCID 1140—
ProductHCID 11031413HCID 1103141346%

Reaction Steps

18-Crown-6 (41.6 g) was added to a toluene (484 ml) solution of trimethyl phosphonoacetate (22.6 ml) in a nitrogen atmosphere. An 11% potassium hexamethyldisilazide (hereinafter referred to as “KHMDS”)/toluene solution (315 ml) was added thereto, and the obtained mixture was stirred for 1 hour. Under ice-cooling, 4-nitroacetophenone (20 g) was added thereto, and the mixture was stirred for 1 hour. After the reaction was over, the reaction was stopped with a saturated ammonium chloride solution. The reaction mixture was separated with ethyl acetate and water. The organic layer was washed three times with water and once with a saturated sodium chloride solution, and then dried over anhydrous sodium sulfate. After the solvent was distilled off, the residue was suspended in methanol (40 ml) and stirred. The precipitated solid was filtered off and washed with cold methanol. Thus, Compound 6a (12.4 g, 46%) was obtained as an opalescent solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855300B2
Source datasetuspto-grants-2010_12
ORD IDord-4e1abc231d0e4d6fb1cb0ef1bce0716c
Source noteuspto-grants-2010_12